Soy Protein Isolate Film by Incorporating Mandelic Acid as Well as Through Fermentation Mediated by Bacillus Subtilis

Soy protein isolate(SPI)biopolymeric films were prepared by adding different contents of mandelic acid(1 to 5%wrt SPI)to glycerol plasticized SPI by solution casting method.Also,SPI was fermented by Bacillus subtilis to get fermented SPI films by solution casting.Molecular mass determination of mandelic acid incorporated and fermented SPI films was carried out by sodium dodecyl sulphate-polyacrylamide gel electrophoresis(SDS-PAGE).Mandelic acid incorporated and fermented SPI films were characterized by Fourier-transform infrared spectroscopy(FT-IR),dynamic mechanical analysis(DMA),tensile strength,water uptake and optical transmittance studies.Results indicated that incorporation of mandelic acid in SPI resulted in high tensile strength(8.03 MPa)and highα-relaxation(Tα)as well as low water uptake.On the other hand,films cannot be prepared from fermented SPI with SPI contents of 8%and 12%.However,film from fermented SPI with 16%SPI content could be prepared but it exhibited low tensile strength(3.18 MPa)and low Tαas well as high water uptake.The resulting mandelic acid incorporated SPI films were also subjected to antimicrobial studies.At all the concentration of mandelic acid,we can easily observe the antimicrobial effect in mandelic acid incorporated SPI films unlike fermented SPI films.This work will be helpful in fabricating antimicrobial SPI film from renewable resources.

Mandelic Acid Single-Crystal Growth:Experiments vs Numerical Simulations

Mandelic acid is an enantiomer of interest in many areas,in particular for the pharmaceutical industry.One of the approaches to produce enantiopure mandelic acid is through crystallization from an aqueous solution.We propose in this study a numerical tool based on lattice Boltzmann simulations to model crystallization dynamics of(S)-mandelic acid.The solver is first validated against experimental data.It is then used to perform parametric studies concerning the effects of important parameters such as supersaturation and seed size on the growth rate.It is finally extended to investigate the impact of forced convection on the crystal habits.Based on there parametric studies,a modification of the reactor geometry is proposed that should reduce the observed deviations from symmetrical growth with a five-fold habit.

Separation of mandelic acid and its derivatives with new immobilized cellulose chiral stationary phase

A new liquid chromatographic method has been developed for the chiral separation of the enantiomers of mandelic acid and their derivatives 2-chloromandelic acid, 4-hydroxymandelic acid, 4-methoxymandelic acid, and 3,4,5-trismethoxymandelic acid. The enantiomers were separated by a CHIRALPAKIC (250 mm×4.6 mm, 5 μm). Mandelic acid, 4-methoxymandelic acid, and 3,4,5-trismethoxymandelic acid were baseline resolved (resolution factor (RS )=2.21, RS =2.14, and RS =3.70, respectively). In contrast, the enantioselectivities between CHIRALPAKIC and 2-chloromandelic acid and 4-hydroxymandelic acid investigated were low. By comparing the chromatographs of mandelic acid enantiomers and mandelic acid spiked with (R)-mandelic acid, it was determined that the first effluent was (R)-mandelic acid.

Synthesis,structure and spectroscopic studies of europium complex with S(+)-mandelic acid

The Eu^3＋ complexes with S（＋）-mandelic acid were synthesized in the form of powders by mixing aqueous solutions of EuCl3, S（＋）-mandelic acid and NaOH in different molar ratios. The powders were characterized by elemental analysis, X-ray powder diffraction （XRPD.） method, Fourier transform infrared （FTIR） and Raman spectroscopy, UV-vis reflectance and luminescence spectra as well as luminescence lifetime measurements. It was found that all studied powders of Eu^3＋ complexes with S（＋）-mandelic acid were isostructural and crystalline and formed compounds with the formula Eu（Man）3（H2O）2.

Molecular Basis for Stereospecific Hydrolysis of Ethyl Mandelate by Thermophilic Esterase

The stereospecific hydrolysis of mandelate can be effectively catalyzed by hyperthermophilic acylpeptide esterase APE 1547（Aeropyrum pernix esterase 1547）. APE 1547 used in this reaction showed a remarkable stereodi-scrimination in favour of R-mandelic acid（99% e.e.） with an enantiomeric ratio E〉200. The results of computer simulation are consistent with the experimental results. It can be inferred that the R-substrate adopted a binding mode productive of the reaction due to the formation of the hydrogen bond at the active site of APE 1547.